Visitor Monitoring Drug History: MAXIDEX
 
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Label and Approval History

Drug Name: MAXIDEX
FDA Application No: (ANDA) 083342
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE
Company: ALCON
 
Label History
 
Labels are not available on this site for MAXIDEX, (ANDA) 083342
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/23/1999 014Chemistry  
9/27/1993 013Labeling  
6/5/1992 012Chemistry in Effect  
2/3/1993 011Chemistry  
9/25/1991 010Chemistry  
2/23/1990 009Chemistry  
9/21/1989 008Labeling  
4/12/1984 006Chemistry  
6/19/1984 005Chemistry  
10/23/1973 000Approval  
 
Therapeutic Equivalents
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